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Study Evaluating Enbrel In Adults With Active Rheumatoid Arthritis In Luxemburg

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Pfizer

Status

Completed

Conditions

Rheumatoid Arthritis

Treatments

Drug: etanercept

Study type

Observational

Funder types

Industry

Identifiers

NCT00195338
0881-101343

Details and patient eligibility

About

The purpose of the study is to determine the long term safety of Enbrel in adults with active rheumatoid arthritis in Luxemburg. This is a post-marketing surveillance study in rheumatology practice patients. All patients initiated with Enbrel will be observed from the start of the study in Feb 2003 for a period of at least 5 years.

Enrollment

25 patients

Sex

All

Ages

17+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Have moderate to severe active rheumatoid arthritis
  • Be aged of 17 years or more
  • Have inadequate response to DMards
  • Give written informed consent
  • Physician decides to prescribe Enbrel

Exclusion criteria

n/a

Trial design

25 participants in 1 patient group

1
Description:
This is an open label, observational study.This is a post-marketing surveillance study in rheumatology practice patients in Luxemburg.Rheumatologists will be asked to document safety and adherence to therapy of Enbrel when given to adults with active rheumatoid arthritis.All patients initiated with Enbrel will be observed.
Treatment:
Drug: etanercept

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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